State

Minnesota product recalls

73,833 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,851
Critical: 1,137
Severe: 2,246
Most recent: 2026-11-04

Of the 7,851 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,246 (29%) are Severe.

Which agencies issued them

These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58351–58375 of 81684

ModerateFDA (Devices)·Z-2544-2015·2015-09-09
Ortho VITROS 5,1 FS Chemistry System Software Recall
Ortho-Clinical Diagnostics is recalling VITROS 5,1 FS Chemistry Systems because a software anomaly may reset user-configured parameters to defaults during installation.
Product
VITROS 5,1 FS Chemistry System, Catalog Number/Product Code 6801375, Unique Device Identifier No. 10758750001132, and VITROS 5,1 FS Chemistry System Refurbished, Catalog Number/Product Code 6801890, Unique Device Identifier No. 10758750001644, IVD --- Ortho Clinical Diagnostics…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2733-2015·2015-09-09
Beckman Coulter Recalls Access Thyroglobulin Assay Reagent Packs
Beckman Coulter is recalling Access Thyroglobulin Assay reagent packs because some may exhibit greater than 10% imprecision at low concentrations.
Product
Access Thyroglobulin Assay; 100 determinations, 2 packs, 50 tests/pack. For the quantitative determination of thyroglobulin levels in human serum and plasma using the Access Immunoassay Systems.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2725-2015·2015-09-09
Transonic Flow Probe Recalled Due to Software Defect
Transonic Systems Inc is recalling 3 mm Flow Probes due to a software defect that causes flow meters to display incorrect status messages.
Product
Transonic Flow Probe, 3 mm, Catalog Number HQC3MP -- Product Usage: to measure flow intra-operatively.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-3073-2015·2015-09-09
HoneyCombs Industries Recalls Expello-C Due to High Coliform Counts
HoneyCombs Industries is recalling 262 bottles of Expello-C because the powdered golden seal ingredient contained coliform bacteria levels exceeding specifications.
Product
Expello-C packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1406-2015·2015-09-09
Qualitest Recalls Lisinopril Tablets for Failed Dissolution Specifications
Vintage Pharmaceuticals is recalling 8,705 bottles of Lisinopril 40 mg tablets because they failed dissolution specifications. The affected lots were distributed nationwide and in Puerto Rico.
Product
Lisinopril Tablets, USP, 40 mg, a) 45-count bottle (NDC 0603-4214-60), b) 500-count bottle (NDC 0603-4214-28), Rx Only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2724-2015·2015-09-09
Transonic Flow Probe Recalled Due to Software Defect in EPROM
Transonic Systems Inc is recalling 2 mm Flow Probes due to programming errors causing incorrect meter readings.
Product
Transonic Flow Probe, 2 mm, Catalog Number HQC2MP -- Product Usage: to measure flow intra-operatively.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2729-2015·2015-09-09
Transonic Flow Probe Recalled Due to Software Defect
Transonic Systems Inc is recalling 6 mm Flow Probes due to programming errors causing incorrect meter readings.
Product
Transonic Flow Probe, 6 mm, Catalog Number HQD6FMV -- Product Usage: to measure flow intra-operatively.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2726-2015·2015-09-09
Transonic Flow Probe Recall Due to Software Defect in EPROM
Transonic Systems Inc is recalling 2 mm Flow Probes due to programming errors causing incorrect meter readings.
Product
Transonic Flow Probe, 2 mm, Catalog Number HQD2FMC -- Product Usage: to measure flow intra-operatively.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2728-2015·2015-09-09
Transonic Flow Probe Recalled Due to Software Defect
Transonic Systems Inc is recalling 4 mm Flow Probes due to software defects causing incorrect meter readings.
Product
Transonic Flow Probe, 4 mm, Catalog Number HQD4FMC -- Product Usage: to measure flow intra-operatively.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2727-2015·2015-09-09
Transonic Flow Probe Recalled Due to Software Defect
Transonic Systems Inc is recalling 3 mm Flow Probes due to software defects causing incorrect readings on flow meters.
Product
Transonic Flow Probe, 3 mm, Catalog Number HQD3FMC -- Product Usage: to measure flow intra-operatively.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-3072-2015·2015-09-09
HoneyCombs Formula L Recalled for Excessive Coliform Bacteria
HoneyCombs Industries is recalling 68 units of Formula L droppers due to coliform counts exceeding specifications.
Product
Formula L packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-3067-2015·2015-09-09
HoneyCombs Recalls Golden Seal Extract Due to High Coliform Count
HoneyCombs Industries is recalling 432 bottles of Golden Seal Extract because the product contained higher levels of coliform bacteria than allowed by specifications.
Product
Golden Seal Extract packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2723-2015·2015-09-09
Transonic Flow Probe Recalled Due to Software Defect
Transonic Systems Inc is recalling 8 mm Flow Probes due to a software defect that causes flow meters to display incorrect error messages.
Product
Transonic Flow Probe, 8 mm, Catalog Number HQC8FMV -- Product Usage: to measure flow intra-operatively.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-3069-2015·2015-09-09
HoneyCombs Formula IM Recalled for Excessive Coliform Bacteria
HoneyCombs Industries is recalling 55 bottles of Formula IM because the powdered golden seal ingredient contained coliform bacteria levels above the specified limit.
Product
Formula IM packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
Category
Food
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1416-2015·2015-09-09
Silarx Lamivudine Oral Solution Recalled for Mismatched Expiration Dates
Silarx Pharmaceuticals is recalling 576 bottles of Lamivudine Oral Solution because the expiration date on the carton does not match the bottle label.
Product
Lamivudine Oral Solution, USP, 10 mg per 1 mL, 240 mL bottle (8 ounces), Rx only, Manufactured by: Silarx Pharmaceuticals, Inc. Carmel, NY 10512, NDC 54838-0566-70
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1405-2015·2015-09-09
Qualitest Recalls Allopurinol Tablets Due to Oversized and Discolored Appearance
Qualitest Pharmaceuticals is recalling 21,552 bottles of 300 mg Allopurinol tablets because some tablets are oversized and discolored.
Product
ALLOPURINOL — ALLOPURINOL (ALLOPURINOL)
Category
Drug
Distribution
Distributed nationwide
SevereUSDA FSIS·120-2015·2015-09-08
Olli Salumeria Americana Recalls Pork Salami Due to Misbranding
Olli Salumeria Americana is recalling pork salami products because the packaging lacks an ingredient list, failing to disclose the presence of sulfites from wine.
Product
OLLI SALUMERIA AMERICANA — Olli Salumeria Americana, LLC Recalls Pork Products Due To Misbranding
Category
Food
Distribution
Distributed nationwide
SevereUSDA FSIS·121-2015·2015-09-08
Schrader Farms Recalls Ground Beef Due To Possible Non-O157 E. Coli Contamination
Schrader Farms is recalling approximately 20 pounds of ground beef sold in Seneca County, New York, due to possible non-O157 E. coli contamination.
Product
Schrader Farms, LLC — Schrader Farms Meat Market Recalls Beef Product Due To Possible Non-O157 E. Coli Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·15E073000·2015-09-08
Cummins Recalls ISB, ISL, and ISX Engines Due to Stalling Risk
Cummins is recalling certain ISB6.7, ISL9, ISX12, and ISX15 engines because a faulty Engine Control Module may cause the engine to stall without warning, increasing crash risk.
Product
ELECTRICAL SYSTEM:IGNITION:MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15V566000·2015-09-08
Hyundai Recalls 2009-2011 Accent Vehicles for Brake Light Switch Defect
Hyundai is recalling approximately 99,500 2009-2011 Accent vehicles because a malfunctioning brake light switch may prevent brake lights from illuminating or disable cruise control.
Product
HYUNDAI — HYUNDAI ACCENT
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·15752·2015-09-08
Rejuvenation Recalls Shaker Chairs and Bar Stools Due to Fall Hazard
Rejuvenation is recalling about 780 Shaker chairs and bar stools because the legs and back can break, causing the user to fall.
Product
Shaker Chairs and Bar Stools
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·15751·2015-09-08
Nestlé Recalls Water Dispensers Due to Fire Hazard
Nestlé Waters North America is recalling about 190 water dispensers because screws holding the heat band can break, causing the unit to overheat and posing a fire hazard.
Product
Water dispensers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·15235·2015-09-08
IKEA Recalls VYSSA SPELEVINK Crib Mattresses for Fire Hazard
IKEA is recalling VYSSA SPELEVINK crib mattresses because they fail to meet federal flammability standards, posing a fire hazard. No injuries have been reported.
Product
VYSSA SPELEVINK crib mattresses
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·15234·2015-09-08
Technical Consumer Products Recalls LED Downlights Due to Shock Hazard
Technical Consumer Products is recalling Connected brand LED downlights because internal wiring can contact metal trim, posing an electrical shock risk.
Product
LED Downlights for Recessed Cans
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·15V562000·2015-09-04
New Flyer Transit Buses Recalled for Potential Steering Loss
New Flyer is recalling 432 transit buses from 2013-2015 because a tie rod clamp may be improperly torqued, risking a loss of steering.
Product
NEW FLYER — NEW FLYER XN40, XN35, XD40, XD60
Category
Vehicle
Distribution
Distributed nationwide